Exploration of a landlocked cenote on Lifou (Loyalty Islands) revealed 37 shells of the cephalopod Nautilus macromphalus Sowerby, 1849, in saltwater on the cenote floor, approximately 40 m below the water surface. The occurrence of these shells is unusual because N. macromphalus is restricted to the open marine waters surrounding the island. All of the shells are mature, and nearly all of them are unbroken, with faded red-brown color stripes. We analyzed seven shells to determine their age. Radiocarbon dating yielded ages of 6380±30 to 7095±30 y BP. The 238U-series radionuclides 210Pb (half-life = 22.3 y) and 226Ra (half-life = 1600 y) also were measured. Two of the samples showed radioactive equilibrium between the nuclides, consistent with the old radiocarbon dates, but the other five samples showed excess 210Pb. When corrected for radioactive decay, the 226Ra activities were much greater than those found in living Nautilus. We conclude that exposure to high activities of 222Rn and 226Ra in the salty groundwater of the cenote altered the activities originally incorporated into the shells. Human placement of the shells in the cavity is rejected based on their radiocarbon age and the geometry of the cenote. The most probable explanation is that the animals entered the flooded karstic system through a connection on the seaward side at approximately 7,000 y BP, during an interval of slowly rising sea level. Unable to find an exit and/or due to anoxic bottom waters, the animals were trapped and died inside. The open connection with the sea persisted for ∼700 y, but after ∼6400 y BP, the connection was lost, probably due to a roof collapse. This is a rare example of Nautilus in a karstic coastal basin and provides a minimum age for the appearance of N. macromphalus in the Loyalty Islands.
Citation: Landman NH, Mapes RH, Cochran JK, Lignier V, Hembree DI, Goiran C, et al. (2014) An Unusual Occurrence of Nautilus macromphalus in a Cenote in the Loyalty Islands (New Caledonia). PLoS ONE 9(12): e113372. https://doi.org/10.1371/journal.pone.0113372
Editor: Steffen Kiel, Universität Göttingen, Germany
Received: March 6, 2014; Accepted: October 25, 2014; Published: December 3, 2014
Copyright: © 2014 Landman et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: Ohio University supported shipping the specimens from New Caledonia to Ohio University. R. H. Mapes and D. I. Hembree were supported by the Baker Grant at Ohio University. V. Lignier was supported by the Laboratoire PPME, Université de la Nouvelle Calédonie. The radiometric analyses were supported by the N.D. Newell Fund at the American Museum of Natural History. The French Federation of Speleology helped support the dive in 2009. Additional funding for the dive in 2011 was provided by the Eramet-Société Le Nickel, a mining company in New Caledonia, and Betco2, a marine transport company operating between Nouméa and the Loyalty Islands. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors received funding for the dive in 2011 from the Eramet-Société Le Nickel, a mining company in New Caledonia, and Betco2, a marine transport company operating between Nouméa and the Loyalty Islands. This funding does not alter the authors' adherence to PLOS ONE policies on sharing data and materials.
Shells of Nautilus macromphalus Sowerby, 1849 , were discovered in a landlocked cenote near the west coast of Lifou in the Loyalty Islands (New Caledonia) during three diving expeditions between 2009 and 2011 (Fig. 1). No evidence of an open connection between the cenote and the sea is visible at this time. Nautilus macromphalus is endemic to these islands and usually occurs at depths between 50 and 500 m , . Drifted shells of this species commonly wash up along the shore , but this is one of the few known occurrences of Nautilus shells in a coastal karstic basin. The abundance and relatively good preservation of the shells allow dating of the specimens to provide information on their origin and the time of appearance of N. macromphalus in the Loyalty Islands.
Map showing location of Lifou within the Loyalty Islands, New Caledonia. The entrance of the Ani e Wee cenote on Lifou (marked with an X) is approximately 200 m from the coast.
Lifou is the largest of the Loyalty Islands and is located 190 km northeast of New Caledonia. It is a raised atoll with coral limestones exposed along the margin and lagoonal biomicrities exposed at the center of the island. It has been uplifted approximately 100 m due to its position on the leading edge of the Australian plate prior to its subduction at the Vanuatu Trench , . During the Pleistocene, an extensive karstic system developed on the island , especially along the coast, where caves periodically became flooded in response to glacioeustatic changes in sea level. The karstic features along the coast comprise anchialine (or anchihaline), habitats, which were defined by Holthuis  as “pools with no surface connection with the sea, containing salt or brackish water, which fluctuates with the tides”. This concept was later modified slightly to emphasize subterranean connections to the sea as well as terrestrial influences , .
C. Goiran received administrative permission to collect Nautilus from the Province des îles Loyauté. She also obtained formal authorization from the Province Sud to export the empty Nautilus shells for scientific purposes. P. Brunet received permission to explore and collect the Nautilus in the cenote from the local chiefs who oversee the area in Lifou. The authors received funding for the dive in 2011 from the Eramet-Société Le Nickel, a mining company in New Caledonia, and Betco2, a marine transport company operating between Nouméa and the Loyalty Islands. This funding does not alter our adherence to PLOS ONE policies on sharing data and materials.
The lake in the cenote can be reached without climbing equipment. Indeed, occasionally, local youth come to bathe there. Nevertheless, security requires the use of ropes to transport heavy equipment. Diving in the cave requires mastering the techniques of cave diving including diving in the dark under a ceiling with a life-line. The location of each shell was recorded with reference to a quadrant system (each square frame is 1 m×1 m). Shells were numbered, mapped, and photographed using the quadrant array. Six quadrants were established, and two to six shells were inventoried in each quadrant. The specimens were labeled to provide information on the sequence in which each shell was collected and the quadrant in which it was collected in, for example, N10QC indicates the tenth Nautilus shell collected, which was in the C quadrant. Locality information for sample ID1 was not recorded.
210Pb and 226Ra analysis
The shells were crushed into fine pieces, and ∼100 g of each shell were sealed in aluminum cans for analysis (leaving a few pieces over for future examination, reposited in the Division of Paleontology, American Museum of Natural History). After a delay of several weeks to ensure the attainment of equilibrium between 226Ra and 222Rn and daughters, the samples were counted on a 3800 mm2 Canberra planar intrinsic germanium gamma detector. Gamma emissions at 46 keV (210Pb) and 352 keV (214Bi) were used to calculate the activities of 210Pb and 226Ra, respectively. NIST SRM 4350B was used to determine the counting efficiency of 226Ra. Solution standards of varying density were prepared to calibrate the 210Pb measurements and correct for sample self-absorption of 210Pb gamma rays.
Following gamma spectrometry, several pieces from each shell were selected for radiocarbon analyses (the samples were destroyed in the process). Samples were converted to graphite, and 14C was measured via accelerator mass spectrometry at the WM Keck Carbon Cycle Accelerator Mass Spectrometry Laboratory (University of California, Irvine). Sample preparation backgrounds were subtracted, based on measurements of 14C-free calcite and normalization standards (OX-1) run with each set of samples. One sample also was rerun by selecting a large shell chip (>1 mm), crushing it coarsely, and then applying a 20–30% acid etch prior to 14C analysis.
The cenote is called “Ani e Wee” (also known as “Ani Angetre Ceu”) by the local indigenous people (Kanaks). It is located 200 m from the east coast of Sandalwood Bay (Baie de Sandal), south of the village of Chépénéhé (Fig. 1). Sandalwood Bay is a broad, shallow embayment and only exceeds a depth of 40 m at a distance of 8 km away from the coastline. The entrance of the cenote is a collapsed depression 30 m in diameter at the bottom of which is a lake 6 m wide, 20 m long, and 20 m deep (Fig. 2). The chasm opens up into a long gallery that forms a dogleg, and then dips down at an angle of 45° extending to a depth of 50 m. The roof of the gallery is covered with speleothems, and the floor is strewn with a scree slope of debris along the entire passageway. The blocks of debris are as much as 1 m in diameter.
Schematic vertical section of the cenote (NNW-SSE) as determined by a dive in 2010. The entrance of the cenote is approximately 30 m in diameter. The Nautilus shells occur between 35 and 45 m. Because of the cenote geometry, a shell thrown into the opening by humans could not have come to rest in its present position.
The cenote contains a lens of fresh water on the surface, brackish water below, and brine at depth (Fig. 2). Closest to the entrance area, the sediments are dark, viscous, and mainly consist of organic matter and detrital carbonate grains. Between depths of 25 m and 35 m, the sediment is light brown and consists of organic matter and carbonate silt. Below 35 m, sediment is sparse. It is light tan, silty to clayey carbonate mud only a few millimeters thick. The three sediment types correspond respectively to fresh water to a depth of ∼25 m (dark organic sediments), brackish water between ∼25 and 35 m (light brown sediments), and marine water below ∼35 m (light tan sediments). The water level shows some variation with the tides, suggesting a subterranean connection with the sea.
Description of Nautilus shells
Altogether, a total of 37 shells of Nautilus macromphalus were observed on the cenote floor between 35 and 45 m below the surface of the water. The shells are oriented randomly with most shells lying on their sides in and among the fallen blocks (Fig. 3D, E). Nearly all of the shells are intact, but at least one of them is damaged, probably from a fallen block. A few millimeters to a few centimeters of sediment partially cover the shells, filling the umbilical opening and body chamber. Some of the shells are cemented to the floor. No living organisms or remains of other marine invertebrates (or vertebrates) are associated with the shells.
A. Live specimen of Nautilus macromphalus from New Caledonia. B, C. Specimens of N. macromphalus from the Ani e Wee cenote with faded red-brown color stripes. D, E. Still frames from a video clip showing specimens of N. macromphalus in situ on the rocky cenote floor. F, G. Scanning electron micrographs of the cross-section and surface, respectively, of the shell wall of a specimen of N. macromphalus from the Ani e Wee cenote.
Seven shells were collected for further analysis. All are mature individuals as indicated by their size (15–16 cm in diameter) and color pattern, with the red-brown color stripes disappearing on the ventral area of the body chamber (Fig. 3B–E). The shells do not exhibit any borings, repaired shell injuries, or evidence of epizoa. No periostracum is present, and the red-brown color stripes are faded, so that the surface of the shell presents a chalky appearance (compare Fig. 3A to 3B, C). In close-up, the shell surface is granular (Fig. 3G), reflecting dissolution of the outer prismatic layer. However, no mineral deposits are present on the surface. In cross-section, the nacreous microstructure of the shell is degraded. The nacreous tablets are slightly fused together, giving the impression of minor dissolution and reprecipitation (Fig. 3F). According to the preservation index of nacre established by Cochran et al. , the PI is 3.5 (good to very good).
The shells were ground up into small pieces for radiocarbon dating. The radiocarbon dates average 6764±30 y BP with a range from 6380±30 to 7095±30 y BP (Fig. 4A; Table 1). Two of the shells each were analyzed twice, and one of the shells was analyzed three times, all with nearly identical results. In addition, one of the samples was re-analyzed after treatment with mild acid to remove any contaminants on the surface and yielded nearly the same result (Fig. 4A). The 238U series radionuclides 210Pb (half-life = 22.3 y) and 226Ra (half-life = 1600 y) were also measured (Fig. 4B; Table 2). One of the samples was measured twice with nearly identical results. Two of the samples show radioactive equilibrium between the nuclides, consistent with the old radiocarbon dates. However, the other five samples show excess 210Pb.
A. Radiocarbon dates range from 6380±30 to 7095±30 y BP. B. Activity ratio of 210Pb/226Ra. Two of the specimens show an activity ratio of approximately 1.0 suggesting an age of >100 years, which is consistent with the old radiocarbon ages. The other specimens show an excess of 210Pb. Correcting the 226Ra activities for decay (∼7000 years) produces values much greater than those observed in living Nautilus. Shells were likely exposed to high activities of 222Rn and 226Ra in the groundwater of the cenote such that 210Pb and 226Ra were adsorbed on the shell surfaces elevating their activities.
The alteration observed in the nacreous microstructure of the Nautilus shells could affect the determination of the radiocarbon age. Mild acid leaching of the surface of one shell sample and re-analysis for radiocarbon yielded no difference in age, suggesting that any alteration is integral to the shell itself and not caused by the precipitation of a surface phase. Indeed, Cochran et al.  demonstrated that as preservation declines in fossil ammonoids and nautiloids, the nacreous tablets begin to fuse together, probably due to the precipitation of SrCO3. The added carbonate may be derived from dissolution and re-precipitation of the shell itself or from the dissolved inorganic carbon (DIC) reservoir in the water surrounding the shells. In the former case, the radiocarbon age would be unaffected, but, in the latter, carbon of a different age would be added to the shell. Because the shell preservation of the Lifou samples is assessed as good-to-very good (PI = 3.5), the added carbonate likely accounts for less than ∼5% of the shell carbon. If the DIC were imprinted with pre-bomb C (fraction modern = 1), then a 5% addition would have produced a radiocarbon age ∼500 y younger than the true age of the shell. In contrast, if the DIC in the cenote is old (e.g. 10,000 y, derived from the carbonate rocks of the island), the alteration would have produced a shell radiocarbon age ∼150 y older than the true age. We therefore conclude that the radiocarbon ages of the shells are within several hundred years of their true ages.
Nautilus secretes its shell with excess 210Pb (half-life = 22.3 y; 210Pb/226Ra >1.0) and with 226Ra activities of 0.04–0.15 dpm/g , . The two shell samples with a 210Pb/226Ra activity ratio of approximately 1.0 suggest an age of >5 half-lives of 210Pb or ≥100 years (Table 2), which is consistent with the old radiocarbon dates of these specimens (Table 1). However, in the other five specimens, the ratio is greater than 1, suggesting a younger age. Correcting the 226Ra (half-life = 1600 y) activities measured in the samples for decay over ∼7000 y produces values much greater than those observed in present-day Nautilus , . The saline groundwaters of a cenote in the Yucatán, Mexico, have very high dissolved 226Ra activities , and a similar situation probably exists in the cenote in Lifou. Activities of dissolved 222Rn also would be elevated in such a system, and decay of 222Rn would produce 210Pb that could be adsorbed onto the surfaces of the shells or be incorporated into the shell wall during alteration. These processes probably altered the 210Pb and 226Ra activities in the shells, and suggest that the use of 210Pb/226Ra disequilibrium is not an appropriate method for dating these specimens.
We conclude that the average age of the shells of Nautilus macromphalus in the cenote is ∼6800 y BP. The question remains of how the shells arrived in the basin. Human placement of the shells in the gallery is rejected for two reasons. The first is the geometry of the cenote (Fig. 2). The cenote entrance opens up to a freshwater lake. Any shell thrown in by hand would have landed at the bottom of the pool at a depth of 20 m and not along the angled passageway where the shells occur. In addition, the first settlers on Lifou probably arrived at approximately 2500 y BP based on radiocarbon dating of hand stencils in nearby caves . Thus, the average radiocarbon age of 6800 y BP predates the arrival of humans.
Today, the circulation of marine waters in the cenote is limited, as indicated by the reduced tidal rise and fall of the water level. However, the ages of the shells indicate that the passageway from the ocean to the cenote was open and accessible to Nautilus. The average date of 6800 y BP approximately coincides with an interval of slowly rising sea level, following the last rapid rise due to glacioeustatic processes (Fig. 9 in ). As a result, the ocean must have flooded the karstic system, perhaps multiple times. The absence of other organisms in the cenote suggests that they either did not enter the passageway, or if they did, they died inside and were dissolved away. The fact that more ancient and younger Nautilus shells have not been recovered suggests that the passageway to the cenote was open for a restricted length of time and then was blocked. This blockage was probably caused by a roof collapse, as indicated by the scree slope of limestone blocks. Similar collapses have been reported in coastal karstic systems elsewhere . We conclude that Nautilus were able to enter what is now the cenote for a span of approximately 700 years.
The specimens may have arrived of their own volition or by post-mortem drift. The excellent preservation of the shells without broken edges or encrusting epizoans suggests that the animals swam rather than floated in. Nevertheless, it is surprising that the Nautilus ventured so far into shallow water so close to shore. However, in New Caledonia, Nautilus have occasionally been observed in shallow water during the austral winter months , , . Willey  noted that “…in Sandal Bay [Sandalwood Bay], Lifou, in the Loyalty Group…Nautilus migrates at night from deep water into as little as three fathoms.” R. Davis (pers. comm., as cited in ) also reported catching a specimen by hand-line at night in Sandal Bay at an apparent depth of less than 5 m. Most of the specimens observed in shallow water are mature , which matches the description of the shells in the cenote. The animals may have been searching for benthic crustaceans such as hermit crabs and lobsters, which have been reported in the crop contents of Nautilus caught between 10 and 30 m . They may also have been attracted by an unusual food item, for example, an animal corpse that fell from the land into the abyss, which they detected by smell. Alternatively, the Nautilus may have taken refuge in the crevices and caves, trying to avoid predators such as turtles, triggerfish, and sharks.
Once in the cavity, the animals might not have been able to find the exit and died of starvation. Alternatively, they may have died due to suffocation from anoxic bottom waters, which have been reported in cenotes on Ouvéa in the Loyalty Islands . Decomposition of the soft body may have caused the shells to float upward, a common phenomenon after death . However, the shells probably did not reach the surface of the freshwater pool because of the cenote geometry. Eventually, such shells would have become waterlogged and sunk to the floor where they accumulated at a depth of 35 to 45 m.
Shells of Nautilus macromphalus also have been reported in the Manev cenote on the east coast of Lifou, near the village of Wé (pers. comm., S. Pujol). They are more completely buried in the sediment and less well preserved than those in the present study. In both the Manev and the Ani e Wee cenotes, the cavities are close to the shore, and must have been flooded by sea level rise during the Holocene.
Although Nautilus is considered a “living fossil,” the actual fossil record of this genus is very poor, making the study of its evolutionary history and migratory pathways difficult. The only record of a fossil Nautilus is a specimen attributed to N. pompilius from the Philippines, which, based on microfossils in the surrounding rock matrix, appears to be early Pleistocene . The maximum age of the specimens in the cenote on Lifou provides a minimum age of the appearance of N. macromphalus in the Loyalty Islands. According to phylogenetic reconstructions based on molecular data, N. macromphalus diverged from the common ancestor of the Nautilus populations in Fiji, Vanuatu, and American Samoa . Our radiocarbon data reveal that this event must have occurred no later than 7100 y BP.
The occurrence of Nautilus macromphalus in a cenote on Lifou in the Loyalty Islands is unusual because this species is restricted to the open marine waters surrounding the islands. Human placement of the shells in the cenote is rejected based on their radiocarbon age and the geometry of the cenote. The well-preserved state of the shells suggests that the specimens entered as live animals from Sandalwood Bay. The radiocarbon dates indicate that this occurred following the last rapid rise of sea level. Once inside the cenote, the animals became trapped and died of starvation or suffocation. The passageway may have persisted for approximately 700 y after which a roof collapse probably blocked the seaward entrance. The radiocarbon analysis indicates that N. macromphalus was present in the Loyalty Islands at least as long ago as 7100 y BP.
We thank Ellen Druffel (University of California, Irvine) for analyzing the samples for radiocarbon and for helping to interpret the results, Christina Heilbrun (Stony Brook University) for assistance with the 210Pb and 226Ra analyses, Kathy Sarg (American Museum of Natural History) for examining the specimens under SEM, and Richard Arnold Davis (College of Mount St. Joseph) and Christian Klug (Universität Zűrich) for carefully reviewing the manuscript and making many helpful suggestions.
Conceived and designed the experiments: NHL RHM JKC VL DIH CG EF PB. Performed the experiments: NHL RHM JKC VL DIH CG EF PB. Analyzed the data: NHL RHM JKC VL DIH CG EF PB. Contributed reagents/materials/analysis tools: NHL JKC. Wrote the paper: NHL RHM JKC VL PB.
- 1. Sowerby GB (1849) Monograph of the genus Nautilus. Thesaurus Conchyliorum 2:463–465.
- 2. Ward PD, Martin AW (1980) Depth distribution of Nautilus pompilius in Fiji and Nautilus macromphalus in New Caledonia. The Veliger 22:259–264.
- 3. Ward PD (1983) Nautilus macromphalus. In: Boyle Peditor. Cephalopod Life Cycles, vol. 1. London: Academic Press. pp. 11–28.
- 4. Mapes RH, Hembree DI, Rasor BA, Stigall A, Goiran C, et al. (2010) Modern Nautilus (Cephalopoda) taphonomy in a subtidal to backshore environment, Lifou (Loyalty Islands). Palaios 25:656–670.
- 5. Marshall JF, Launay J (1978) Uplift rates of the Loyalty Islands as determined by 230Th/234U dating of raised coral terraces. Quaternary Research 9:186–192.
- 6. Genthon P, Wirrmann D, Hoibian T, Allenbach M (2008) Steady water level and temperature in a karstic system: the cave of the coral Lifou Island (SW Pacific). Comptes Rendus Geoscience 340:513–522.
- 7. Thomas C (1987) Grottes de Nouvelle Calédonie: Nouméa: Sophocle. pp. 1–52.
- 8. Holthuis LB (1973) Caridean shrimps found in land-locked saltwater pools at four Indonesian West Pacific locations. Zool. Verhand. 128:1–48.
- 9. Stock JH, Iliffe TM (1995) Melitidae (Crustacea, Amphipoda) from anchihaline limestone caves in New Caledonia. Contributions to Zoology 65:245–269.
- 10. Stock JH, Iliffe TM, Williams D (1986) The concept “anchialine” reconsidered. Stygologia 2:90–92.
- 11. Cochran JK, Kallenberg K, Landman NH, Harries PJ, Weinreb D, et al. (2010) Effect of diagenesis on the Sr, O, and C isotope composition of late Cretaceous mollusks from the Western Interior Seaway of North America. American Journal of Science 310:69–88.
- 12. Cochran JK, Rye DM, Landman NH (1981) Growth rate and habitat of Nautilus pompilius inferred from radioactive and stable isotope studies. Paleobiology 7:469–480.
- 13. Mapes RH, Landman NH, Cochran K, Goiran C, Richer de Forges B, et al. (2010) Early taphonomy and significance of naturally submerged Nautilus shells from the New Caledonia region. Palaios 25:597–610.
- 14. Gonneea ME, Charette MA, Liu Q, Herrera-Silveira JA, Morales-Ojeda SM (2014) Trace element geochemistry of groundwater in a karst subterranean estuary (Yucatan Peninsula, Mexico). Geochimica et Cosmochimica Acta. 132:31–49.
- 15. Sand C, Valladas H, Cachier H, Tisnérat-Laborde N, Arnold M, et al. (2006) Oceanic rock art: first direct dating of prehistoric stencils and paintings from New Caledonia (Southern Melanesia). Antiquity 80:523–529.
- 16. van Hengstrum PJ, Scott DB, Gröcke DR, Charette MA (2011) Sea level controls sedimentation and environments in coastal caves and sinkholes. Marine Geology 286:35–50.
- 17. Smart PL, Beddows PA, Coke J, Doerr S, Smith S, et al. (2006) Cave development on the Caribbean coast of the Yucatan Peninsula, Quintana Roo, Mexico. In: Harmon RS, Wicks Ceditors. Perspectives on karst geomorphology, hydrology, and geochemistry—A tribute volume to Derek C. Ford and William B. White. Geological Society of America Special Paper 404. pp. 105–128.
- 18. Saunders WB, Ward PD (1987) Ecology, distribution, and population characteristics of Nautilus. In: Saunders WB, Landman NHeditors. Nautilus: The Biology and Paleobiology of a Living Fossil. New York, Plenum Press. pp. 137–162.
- 19. Willey A (1899) General account of a zoological expedition to the South Seas during the years 1894–1897. Proceedings of the Zoological Society of London 1899:7–9.
- 20. Ward PD, Wicksten MK (1980) Food sources and feeding behavior of Nautilus macromphalus. The Veliger 23:119–124.
- 21. Iliffe TM, Sarbu S (1990) Anchialine caves and cave fauna of the South Pacific. National Speleological Society, NSS News 48:88–96.
- 22. Chamberlain JA Jr, Ward PD, Weaver JS (1981) Post-mortem ascent of Nautilus shells: Implications for cephalopod paleobiogeography. Paleobiology 47:494–509.
- 23. Wani R, DeOcampo RSP, Aguilar YM, Zapeda MA, Kurihara Y, et al. (2008) First discovery of fossil Nautilus pompilius Linnaeus, 1758 (Nautilidae, Cephalopoda) from Pangasinan, northwestern Philippines. Paleontological Research 12:89–95.
- 24. Bonacum J, Landman NH, Mapes RH, White MM, White A-J, et al. (2011) Evolutionary radiation of present-day Nautilus and Allonautilus: American Malacological Bulletin. 29:77–93.
- 25. Stuiver M, Polach HA (1977) Reporting of 14C data. Radiocarbon 19:355–363.